Involvement of the pathway phosphatidylinositol-3-kinase/AKT-1 in the establishment of the survival response to ionizing radiation

被引:42
作者
Cataldi, A
Zauli, G
Di Pietro, Z
Castorina, S
Rana, R
机构
[1] Univ Chieti, Fac Med & Chirurg, Dipartimento Biomorfol, I-66100 Chieti, Italy
[2] Catania Univ, Ist Anat Umana, Fac Med & Chirurg, Catania, Italy
关键词
PI-3-kinase; AKT-1; survival; ionizing radiation;
D O I
10.1016/S0898-6568(01)00147-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ionizing radiation is one of the agents inducing activation of DNA repair, cell cycle arrest, apoptosis and cell death. Here we report evidence for an enhanced activity of DNA polymerase beta, one of the repair enzymes, concomitant to the activation of the pathway phosphatidylinositol-3-kinase/AKT-1 (PI-3-kinase/AKT-1), which delivers a survival signal in Friend erythroleukemia cells exposed to 15 Gy. Significantly, the preincubation of the cellls with PI-3-kinase inhibitors wortmannin and LY 294002, disactivating this pathway, sensitizes the cells to ionizing radiation by further reducing the rate of proliferation without substantial variations of the number of dead cells: Thus, we suggest a role for these enzymes in maintaining survival programs upon exposure to ionizing radiation and in giving to these cells a chance to recover from this stress. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:369 / 375
页数:7
相关论文
共 49 条
[21]   The PI 3-kinase/Akt signaling pathway delivers an anti-apoptotic signal [J].
Kennedy, SG ;
Wagner, AJ ;
Conzen, SD ;
Jordan, J ;
Bellacosa, A ;
Tsichlis, PN ;
Hay, N .
GENES & DEVELOPMENT, 1997, 11 (06) :701-713
[22]   DNA polymerase ε catalytic domains are dispensable for DNA replication, DNA repair, and cell viability [J].
Kesti, T ;
Flick, K ;
Keränen, S ;
Syväoja, JE ;
Wittenberg, C .
MOLECULAR CELL, 1999, 3 (05) :679-685
[23]   IONIZING-RADIATION STIMULATES A GRB2-MEDIATED ASSOCIATION OF THE STRESS-ACTIVATED PROTEIN-KINASE WITH PHOSPHATIDYLINOSITOL 3-KINASE [J].
KHARBANDA, S ;
SALEEM, A ;
SHAFMAN, T ;
EMOTO, Y ;
TANEJA, N ;
RUBIN, E ;
WEICHSELBAUM, R ;
WOODGETT, J ;
AVRUCH, J ;
KYRIAKIS, J ;
KUFE, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (32) :18871-18874
[24]  
KIMURA K, 1994, J BIOL CHEM, V269, P18961
[25]   A specific product of phosphatidylinositol 3-kinase directly activates the protein kinase Akt through its pleckstrin homology domain [J].
Klippel, A ;
Kavanaugh, WM ;
Pot, D ;
Williams, LT .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (01) :338-344
[26]  
Krasilnikov M, 1999, MOL CARCINOGEN, V24, P64, DOI 10.1002/(SICI)1098-2744(199901)24:1<64::AID-MC9>3.0.CO
[27]  
2-2
[28]   THE BIOCHEMISTRY OF PROGRAMMED CELL-DEATH [J].
KROEMER, G ;
PETIT, P ;
ZAMZAMI, N ;
VAYSSIERE, JL ;
MIGNOTTE, B .
FASEB JOURNAL, 1995, 9 (13) :1277-1287
[29]  
Leadon, 1996, Semin Radiat Oncol, V6, P295, DOI 10.1016/S1053-4296(96)80025-7
[30]   PKB/Akt: connecting phosphoinositide 3-kinase to cell survival and beyond [J].
Marte, BM ;
Downward, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (09) :355-358